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Acetonitrile → 1-[4-(trifluoromethyl)phenyl]-4-Piperidinone

HRID 1382852
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1382852
F[C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][CH:3]=1.C([O-])([O-])=O.[K+].[K+].O1[C:22]2([CH2:27][CH2:26][NH:25][CH2:24][CH2:23]2)[O:21]CC1.C(#N)C>O>[F:9][C:8]([F:11])([F:10])[C:5]1[CH:6]=[CH:7][C:2]([N:25]2[CH2:26][CH2:27][C:22](=[O:21])[CH2:23][CH2:24]2)=[CH:3][CH:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6342AcetonitrileHCID 11430Potassium CarbonateHCID 674351,4-Dioxa-8-azaspiro(4.5)decaneHCID 67873Benzene, 1-fluoro-4-(trifluoromethyl)-

Produkt 1

HCID 212736221-[4-(trifluoromethyl)phenyl]-4-PiperidinoneAusbeute 2,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962
Water
Lösungsmittel

Versuchsvorschrift

A mixture of 25 g (0.1523 mol) of p-fluorobenzotrifluoride, 31 g (0.224 mol) of K2CO3, 65 g (0.4539 mol) of 1,4-dioxa-8-azaspiro[4.5]decane, and 150 ml of acetonitrile is stirred at reflux for 3 days. The reaction mixture is cooled, diluted with water, and extracted with methylene chloride. The combined extracts are washed with water, dried over Na2SO4 and concentrated in vacuo. The residue, 600 ml of 10% sulfuric acid solution and 300 ml of tetrahydrofuran is stirred at ambient temperature for 7 days, diluted with water and extracted with methylene chloride. The extracts are washed with brine, dried over Na2SO4, and concentrated in vacuo. Trituration with ether gives 0.9 g of title compound: IR (KBr) 1715, 1610, 1520 and 1330 cm-1 ; NMR (CDCl3) δ7.55 (d, 2H), 6.95 (d, 2H)m 3.73 (t, 4H), and 2.59 (t, 4H).

Aufarbeitung

  1. temperatureat reflux for 3 days
  2. temperatureThe reaction mixture is cooled
  3. extractionextracted with methylene chloride
  4. washThe combined extracts are washed with water
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo
  7. stirringThe residue, 600 ml of 10% sulfuric acid solution and 300 ml of tetrahydrofuran is stirred at ambient temperature for 7 days
  8. additiondiluted with water
  9. extractionextracted with methylene chloride
  10. washThe extracts are washed with brine
  11. dry with materialdried over Na2SO4
  12. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d0d057e655b947ca951ed6ff2be6b8d0
Quelldatensatz
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04808612

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